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NGF 和 BDNF 依赖性背根神经节感觉神经元采用不同的退行性信号机制。

NGF-Dependent and BDNF-Dependent DRG Sensory Neurons Deploy Distinct Degenerative Signaling Mechanisms.

机构信息

Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Quebec H3A 2B4, Canada.

Department of Biology, University of British Columbia Okanagan, Kelowna, British Columbia V1V 1V7, Canada.

出版信息

eNeuro. 2021 Jan 21;8(1). doi: 10.1523/ENEURO.0277-20.2020. Print 2021 Jan-Feb.

Abstract

The nerve growth factor (NGF) and brain-derived neurotrophic factor (BDNF) are trophic factors required by distinct population of sensory neurons during development of the nervous system. Neurons that fail to receive appropriate trophic support are lost during this period of naturally occurring cell death. In the last decade, our understanding of the signaling pathways regulating neuronal death following NGF deprivation has advanced substantially. However, the signaling mechanisms promoting BDNF deprivation-induced sensory neuron degeneration are largely unknown. Using a well-established culture model of dorsal root ganglion (DRG), we have examined degeneration mechanisms triggered on BDNF withdrawal in sensory neurons. Our results indicate differences and similarities between the molecular signaling pathways behind NGF and BDNF deprivation-induced death. For instance, we observed that the inhibition of Trk receptors (K252a), PKC (Gö6976), protein translation (cycloheximide; CHX), or caspases (zVAD-fmk) provides protection from NGF deprivation-induced death but not from degeneration evoked by BDNF-withdrawal. Interestingly, degeneration of BDNF-dependent sensory neurons requires BAX and appears to rely on reactive oxygen species (ROS) generation rather than caspases to induce degeneration. These results highlight the complexity and divergence of mechanisms regulating developmental sensory neuron death.

摘要

神经生长因子 (NGF) 和脑源性神经营养因子 (BDNF) 是神经系统发育过程中特定感觉神经元所需的营养因子。在这段自然发生的细胞死亡期间,未能接收到适当营养支持的神经元会丢失。在过去的十年中,我们对调节 NGF 剥夺后神经元死亡的信号通路的理解有了很大的进展。然而,促进 BDNF 剥夺诱导的感觉神经元变性的信号机制在很大程度上尚不清楚。我们使用已建立的背根神经节 (DRG) 培养模型,研究了 BDNF 撤去后感觉神经元引发的变性机制。我们的结果表明,NGF 和 BDNF 剥夺诱导的死亡背后的分子信号通路存在差异和相似之处。例如,我们观察到,Trk 受体抑制剂 (K252a)、PKC 抑制剂 (Gö6976)、蛋白质翻译抑制剂 (环己酰亚胺;CHX) 或半胱天冬酶抑制剂 (zVAD-fmk) 提供了对 NGF 剥夺诱导的死亡的保护,但不能防止 BDNF 撤去引起的变性。有趣的是,BDNF 依赖性感觉神经元的变性需要 BAX,并且似乎依赖于活性氧 (ROS) 的产生而不是半胱天冬酶来诱导变性。这些结果突出了调节发育中感觉神经元死亡的机制的复杂性和分歧。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb50/7877462/8fb13d83d3cc/SN-ENUJ200339F001.jpg

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